Furosemide analogues as potent inhibitors of the new permeability pathways of Plasmodium falciparum-infected human erythrocytes

Molecular and Biochemical Parasitology

Volumn 133, Issue 2, 2004, Pages 315-318

  Staines, Henry M ^a   Dee, Belinda C ^a   O'Brien, Martin ^a   Lang, Hans Jochen ^b   Englert, Heinrich ^b   Horner, Heather A ^a   Ellory, J Clive ^a   Kirk, Kiaran ^c  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b SANOFI AVENTIS DEUTSCHLAND GMBH   (Germany)

^c AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

Channel; Choline; Erythrocyte; Malaria; Membrane; Transport

Indexed keywords

ANION; ANTIPROTOZOAL AGENT; BUMETANIDE; CHOLINE; CLOMIFENE; FUROSEMIDE; H 105; H 106; H 120; H 131; H 156; H 157; H 158; H 159; H 18; H 19; H 59; MEFLOQUINE; TAMOXIFEN; UNCLASSIFIED DRUG;

ANION TRANSPORT; ARTICLE; CONTROLLED STUDY; DOSE RESPONSE; DRUG EFFECT; DRUG POTENCY; DRUG STRUCTURE; ERYTHROCYTE; HUMAN; HUMAN CELL; IC 50; INCUBATION TIME; ISOTOPE LABELING; MALARIA; NONHUMAN; PARASITISM; PERMEABILITY; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; TROPHOZOITE;

PLASMODIUM FALCIPARUM;

EID: 0347418183     PISSN: 01666851     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molbiopara.2003.10.009     Document Type: Article

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